Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0001-2022 — RAPTAR Laser Range Finders

U.S. FDA — Device Enforcement · United States · 2021-04-21 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0001-2022
Date of alert
2021-04-21
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Potomac River Group, Corp.
Product category
device
Product type
Devices
Reported risk: RAPTAR units are capable of being field modified to enable the use of the higher power visible and IR laser pointers and the IR Illuminator.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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